A NONPROFIT SINCE 2006

About MSCDA

MSCDA affairs are governed by a Board of Directors with day-to-day operations being facilitated by various other volunteers led by Petronella Barrow.
The Maryland Sickle Cell Disease Association, Inc. (MSCDA) is a 501 (c)(3), tax exempt non profit organization that was incorporated in 2006. MSCDA was formed by concerned parents and interested individuals seeking to improve the lives of persons affected by sickle cell disease in Maryland. MSCDA seeks to work collaboratively with patients, families, healthcare providers, federal and state agencies and other community based organizations to promote advocacy, education, research and excellent healthcare delivery.
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MSCDA Team

MSCDA affairs are governed by a Board of Directors with day-to-day operations being facilitated by various other volunteers led by Petronella Barrow.

MSCDA Board of Directors

Derek Robertson
President
Benjamin Joseph
Vice President
Shantá Robertson
Secretary
L-R: Derek Robertson, Shanta Robertson, Petronella Barrow, Ben Joseph
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We'd Love to Hear from You

Whether you are looking to learn more about our services, and how we can help, or you’re looking for volunteer opportunities, to make a donation, or have any questions about the Maryland Sickle Cell Disease Association, please reach out!
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Time to Register!

MSCDA 2021:
Sickle Cell Education Day

Join us for this year’s virtual event!